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Gene expression analysis of the late embryonic mouse cerebral cortex using DNA microarray: identification of several region- and layer-specific genes.

机译:使用DNA芯片对晚期胚胎小鼠大脑皮质进行基因表达分析:鉴定几个区域和层特异性基因。

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The mammalian neocortex develops layer organizations with regional differences represented by expression of multiple genes at embryonic stages. These genes could play important roles in the formation of areal cyto-architecture, yet, the number of genes identified so far is not sufficient to explain such intricate processes. Here we collected five regions--the medial, dorsal, lateral, rostral and occipital--from the dissected E16.5 mouse cerebral cortex and performed extensive gene expression analysis using the Affymetrix U74Av2 array with probes for 12,500 genes. After relative quantitative analysis, 34, 33 and 15 genes were selected as highly expressed genes in the medial, dorsal and lateral regions, respectively. The combination of GeneChip system, real-time quantitative reverse transcription polymerase chain reaction and in situ hybridization analyses allowed the successful identification of seven genes from the dorsal region (Neuropeptide Y, Wnt7b, TGF-beta RI, Nrf3, Bcl-6, MT4-MMP and Rptp kappa),three genes from the medial region (Hop-pending, HtrA and Crystallin), and three genes from the lateral region (Somatostatin, Ngef and Fxyd7). Particularly, all seven genes identified in the dorsal region demarcated the future somatosensory and auditory areas in the cortical plate with high rostrolateral-low caudomedial gradation. Their expression patterns were not uniform, but delineated either the superficial or the deep layer in the cortical plate. Furthermore, the regional expression pattern of Neuropeptide Y was shifted rostrally and the layer specificity was disorganized in the Pax6-deficient mice. Our results provide new information about a subclass of regionally expressed genes in the cortical plate at the late embryonic stage, which may help understand the molecular mechanisms of neocortical arealization.
机译:哺乳动物的新皮层发育具有区域差异的层组织,其在胚胎阶段表达多个基因。这些基因可能在区域细胞结构的形成中起重要作用,但是,迄今为止鉴定出的基因数量不足以解释这种复杂的过程。在这里,我们从解剖的E16.5小鼠大脑皮层收集了五个区域-内侧,背侧,外侧,延髓和枕骨,并使用Affymetrix U74Av2阵列和12500个基因的探针进行了广泛的基因表达分析。经过相对定量分析后,分别选择了34、33和15个基因作为内侧,背侧和外侧区域的高表达基因。通过将GeneChip系统,实时定量逆转录聚合酶链反应和原位杂交分析相结合,可以成功鉴定背侧区域的七个基因(神经肽Y,Wnt7b,TGF-βRI,Nrf3,Bcl-6,MT4- MMP和Rptp kappa),来自内侧区域的三个基因(Hop-pending,HtrA和Crystallin)和来自外侧区域的三个基因(Somatostatin,Ngef和Fxyd7)。特别地,在背侧区域中鉴定出的所有七个基因以较高的rosrolateral-低caudomedial渐变来划分了皮质板中未来的体感和听觉区域。它们的表达方式不统一,但在皮层板的表层或深层都有描绘。此外,神经肽Y的区域表达模式向后移位,并且在Pax6缺陷小鼠中层特异性混乱。我们的研究结果提供了有关胚胎后期皮质板中区域表达基因的一个子类的新信息,这可能有助于了解新皮质区域化的分子机制。

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